Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.810 0.667 3 1995 2013
dbSNP: rs118203906
rs118203906
F5
2 0.925 0.080 1 169555299 missense variant C/G snv 2.3E-04 7.7E-05 0.800 1.000 1 2010 2010
dbSNP: rs118203911
rs118203911
F5
2 0.925 0.080 1 169552693 missense variant A/G snv 0.800 1.000 1 2010 2010
dbSNP: rs118203912
rs118203912
F5
1 1.000 0.080 1 169560701 stop gained C/A snv 0.700 0
dbSNP: rs1453479152
rs1453479152
F5
1 1.000 0.080 1 169544434 missense variant A/G snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs751377893
rs751377893
F5
65 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2018 2018